ConMed recalls 12mm AirSeal Access Ports with potential overpressure alerts. Affected units have specific catalog numbers and production dates. Consumers should contact ConMed for details.
Potential for overpressure alerts.
ConMed is recalling 12mm AirSeal Access Ports and Obturators that may cause overpressure alerts. This could lead to equipment malfunction during medical procedures. The recall affects specific units with catalog number iASB12-100 and production dates from June 2024 to January 2026.
The device may generate overpressure alerts during medical procedures, which could cause equipment malfunction. This is a potential risk in laparoscopic surgery where precise pressure control is critical. However, the hazard is not described as causing serious injury in normal use.
Medical professionals using the ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip during laparoscopic surgery are most at risk. The recall applies to specific units produced between June 2024 and January 2026.
Check for catalog number iASB12-100 on the product. Affected units were manufactured from June 2024 to January 2026 and have specific lot numbers listed in the recall notice.
Look for catalog number iASB12-100 and lot numbers listed in the recall notice to confirm if your unit is affected.
The product may generate overpressure alerts during medical procedures, which could cause equipment malfunction.
Check for catalog number iASB12-100 and lot numbers from June 2024 to January 2026 as listed in the recall notice.
The recall does not specify a remedy, so contact ConMed directly for further instructions.
We’ve drafted a message you can send ConMed to request your refund or repair — edit it as you like.
Subject: Recall Z-2466-2026 — ConMed ConMed Hello, I own a ConMed that is covered by recall Z-2466-2026 from ConMed. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
